EP0534358B1 - Méthode pour la production d'un produit moulé de mousse de polyuréthane à peau intégrale - Google Patents

Méthode pour la production d'un produit moulé de mousse de polyuréthane à peau intégrale Download PDF

Info

Publication number
EP0534358B1
EP0534358B1 EP92116164A EP92116164A EP0534358B1 EP 0534358 B1 EP0534358 B1 EP 0534358B1 EP 92116164 A EP92116164 A EP 92116164A EP 92116164 A EP92116164 A EP 92116164A EP 0534358 B1 EP0534358 B1 EP 0534358B1
Authority
EP
European Patent Office
Prior art keywords
reacting mixture
mold
cavity
polyurethane foam
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92116164A
Other languages
German (de)
English (en)
Other versions
EP0534358A1 (fr
Inventor
Akira c/o TOYODA GOSEI Technical Center Mabuchi
Osamu c/o TOYODA GOSEI Tech. Center Yamanaka
Naoyuki c/o TOYODA GOSEI Tech. Center Kumagai
Satoru c/o TOYODA GOSEI Tech. Center Ono
Motoshi c/o TOYODA GOSEI Tech. Center Matsuura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyoda Gosei Co Ltd
Original Assignee
Toyoda Gosei Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyoda Gosei Co Ltd filed Critical Toyoda Gosei Co Ltd
Publication of EP0534358A1 publication Critical patent/EP0534358A1/fr
Application granted granted Critical
Publication of EP0534358B1 publication Critical patent/EP0534358B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/58Moulds
    • B29C44/588Moulds with means for venting, e.g. releasing foaming gas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/3402Details of processes or apparatus for reducing environmental damage or for working-up compositions comprising inert blowing agents or biodegradable components
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/60Measuring, controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2075/00Use of PU, i.e. polyureas or polyurethanes or derivatives thereof, as moulding material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S425/00Plastic article or earthenware shaping or treating: apparatus
    • Y10S425/812Venting

Definitions

  • the present invention relates to a method for producing an integral skin polyurethane foam having a non-porous, solid layer on its surface.
  • the method is suitable for the production of polyurethane foams by so-called reaction injection molding (RIM hereinafter).
  • RIM reaction injection molding
  • Examples of the polyurethane foams include automotive parts such as steering wheels, steering wheel pads, instrument panels, console box lids, glove box lids, headrests, armrests, and air spoilers.
  • polyurethane foams is an integral skin semi-rigid polyurethane foam. It is produced in the following manner from a long-chain polyol having a molecular weight of the order of thousands, a low-molecular polyol having a molecular weight of the order of tens to hundreds, a catalyst, a pigment, a blowing agent (trichlorofluoromethane or freon-11 or simply freon hereinafter), and an isocyanate. All the components except isocyanate are preliminarily mixed to give a polyol mixture. The polyol mixture is mixed with the isocyanate by a mixing head in a prescribed ratio to give a reacting mixture. Finally, the reacting mixture is injected into a mold cavity made of a highly heat-conductive material, so that it expands in the mold cavity.
  • the polyol mixture and isocyanate Upon injection into the mold cavity, the polyol mixture and isocyanate undergo the urethane-forming reaction, which is exothermic enough to vaporize the fleon in the reacting mixture into a myriad of bubbles.
  • the reacting mixture slowly expands and flows in the mold cavity, expelling the air from the vent hole of the mold cavity when it has reached the vent hole.
  • the urethane-forming reaction and the vaporization of freon take place simultaneously, sustaining a myriad of freon bubbles.
  • the consequence of the reaction is the formation of a highly expanded core at the center of the mold cavity.
  • the reacting mixture close to the walls of the mold cavity undergoes the urethane-forming reaction more slowly than that at the center because the reaction heat dissipates through the walls of the mold cavity The slower the reaction, the less the reaction heat. This suppresses the vaporization of freon and hence generates a less number of freon bubbles. Freon bubbles are compressed or collapsed by the internal foaming pressure.
  • the EP-A-0 006 381 discloses a process for producing a polyurethane foam which comprises feeding a reaction mold with polyurethane polymerization precursors, then plugging the mold, and then evacuating the mold for expanding the reaction mixture in the evacuated mold cavity without any troublesome blowing agent like freon.
  • the present invention was completed to solve the above-mentioned problems. It is an object of the present invention to provide a new method for producing an integral skin polyurethane foam efficiently with a minimum of loss of the reacting mixture, without using troublesome freon or any other blowing agent, said integral skin polyurethane foam having a better appearance and feel and better physical properties than those which are produced by using freon.
  • the process for producing an integral skin polyurethane foam according to claim 1 is provided.
  • the apparatus for producing an integral skin polyurethane foam comprises a mold having a cavity and a vent, a vacuum chamber communicating with the cavity through the vent, a vacuum pump to evacuate the cavity through the vacuum chamber, and a sight glass attached to the vacuum chamber so as to make the vicinity of the vent visible from the outside of the vacuum chamber.
  • Fig. 1 is a half sectional view showing the vacuum chamber and mold (in the open position) used in the first example of the present invention.
  • Fig. 2 is a half sectional view showing RIM operation under way, with the mold closed, in the apparatus as shown in Fig. 1.
  • Fig. 3 is a sectional view taken along line III-III of Fig. 2.
  • Fig. 4 is a partly enlarged sectional view showing a steering wheel pad produced by the apparatus shown in Fig. 1.
  • Fig. 5 is a schematic diagram showing the mixing unit for the reacting mixture.
  • Fig. 6 is a sectional view showing the vacuum chamber and mold (in the open position) used in the second example of the present invention.
  • Fig. 7 is a plan view showing the lower casing of the vacuum chamber and the movable half of the mold (in the open position) in the apparatus as shown in Fig. 6.
  • Fig. 8 is a sectional view showing RIM operation under way, with the mold closed, in the apparatus as shown in Fig. 6.
  • Fig. 9 is a side view showing RIM operation under way, with the mold closed, in the apparatus as shown in Fig. 6.
  • Fig. 10 is a sectional view of the sight glass in the apparatus as shown in Fig. 6.
  • Fig. 11 is a sectional view of the apparatus as shown in Fig. 6, with the mold opened for the demolding of the steering wheel.
  • Fig. 12 is a partly enlarged sectional view of the steering wheel as shown in Fig. 11.
  • Fig. 13 is a graph showing the relationship between the tensile strength of the covering of the steering wheel and the water content in the polyol mixture.
  • Fig. 14 is a graph showing the relationship between the tear strength of the covering of the steering wheel and the water content in the polyol mixture.
  • Fig. 15 is a graph showing the relationship between the thickness of the skin of the steering wheel and the pressure in the cavity.
  • Fig. 16 is a sectional view showing another example of the mold.
  • Fig. 17 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 0.665 kPa (5 Torr).
  • Fig. 18 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 1.596 kPa (12 Torr).
  • Fig. 19 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 1.995 kPa (15 Torr).
  • Fig. 20 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 2.66 kPa (20 Torr).
  • Fig. 21 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 3.99 kPa (30 Torr).
  • Fig. 22 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 6.65 kPa (50 Torr).
  • Fig. 23 is a sectional photomicrograph showing the covering of the steering wheel produced with the pressure in the cavity adjusted to 13.3 kPa (100 Torr).
  • Fig. 24 is a sectional photomicrograph showing the covering of the steering wheel produced in the conventional fleon-based foaming.
  • the process for producing an integral skin polyurethane foam comprises expanding a reacting mixture containing substantially no blowing agent in an evacuated mold cavity.
  • the phrase "containing substantially no blowing agent” means that the reacting mixture is not deliberately incorporated with any blowing agent (including freon, methylene chloride, water, and fine bubbles) for the purpose of blowing or blowing control.
  • the reacting mixture may contain slight amounts of various gases which are originally present therein, slight amounts of air entrapped inevitably thereby during cycling, and slight amounts of moisture absorbed inevitably thereby.
  • the phrase also means that the reacting mixture may contain a variety of blowing agents in such small amounts that they hardly affect the blowing control.
  • the water content (due to the inevitable moisture absorption) in the polyol mixture should preferably be limited to 0.4 wt%. With a water content in excess of 0.4 wt%, the polyol mixture will partly remain unreacted on account of reaction between the water and part of the isocyanate. This results in a polyurethane foam poor in physical properties such as tensile strength and tear strength.
  • the extent to which the mold cavity is evacuated varies depending on the kind and desired expansion ratio of the polyurethane foam to be produced. For the production of steering wheels, it is desirable to evacuate the mold cavity to 6.65 kPa (50 Torr) or below in order to form a skin which should have a soft feel as well as a firm feel.
  • reaction rate of the reacting mixture it is desirable to control the reaction rate of the reacting mixture such that the reacting mixture reaching the vent hole cures to seal the vent hole.
  • a lower reaction rate will result in a large amount of the reacting mixture blowing off from the vent hole.
  • a higher reaction rate will cause molding defects such as short shot, pin-holes, and voids.
  • the reacting mixture Once injected into the mold cavity, the reacting mixture rapidly expands and flows under reduced pressure irrespective of the progress of the urethane-forming reaction. This causes the reacting mixture to reach the vent in a much shorter time than in the conventional process. For the reacting mixture to cure when it has reached the vent hole, it is necessary that the reaction rate of the reacting mixture be much higher than in the conventional process.
  • a means to increase the reaction rate is by increasing the amount of the catalyst or by increasing the temperature of the reacting mixture. (The latter means is possible because no freon is used in the present invention.)
  • the method of the present invention is suitable for producing a polyurethane foam around a core metal previously placed in the mold cavity. It is most suitable for the production of steering wheels, with an integral skin polyurethane foam covering a core metal (at least the ring part thereof) placed in the mold cavity.
  • the apparatus for producing an integral skin polyurethane foam comprises a mold having a cavity and a vent hole, a vacuum chamber communicating with the cavity through the vent, a vacuum pump to evacuate the cavity through the vacuum chamber, and a sight glass attached to the vacuum chamber so as to make the vicinity of the vent hole visible from the outside of the vacuum chamber.
  • the vacuum chamber may be a space of an evacuated box surrounding the mold cavity or a space which is formed, when the mold is closed, by the groove in the periphery of the mold cavity.
  • the reacting mixture is injected into the evacuated mold cavity.
  • the reacting mixture contains substantially no blowing agent, it contains slight amounts of gases originally present therein and absorbed inevitably by it during its cycling. Under reduced pressure, these gases rapidly vaporize, causing the reacting mixture to expand rapidly in a very short time. As the result, the reacting mixture flows in the cavity and fills the cavity. Simultaneously with the expansion, the reacting mixture undergoes the exothermic urethane-forming reaction which brings about curing.
  • the reacting mixture in contact with the inner surface of the mold cavity permits heat to dissipate through the walls of the mold cavity. This heat dissipation makes the urethane-forming reaction slow relative to that at the center and hence prevents the reacting mixture from becoming viscous.
  • the gas bubbles near the inner surface of the mold cavity rupture easily under reduced pressure, and the released gas is removed. Thus there is formed a non-porous solid skin containing even very few minute bubbles.
  • the evacuated cavity helps avoid such defects as pinholes, voids, and short shot. Unlike the conventional foaming by freon, this obviates the necessity of over-packing the reacting mixture to form the skin and to ensure the complete filling and air escape, which leads to the reduction of material loss. In this way, it is possible to produce a superior polyurethane foam composed of a highly expanded core and a solid skin.
  • the foaming due to the expansion of the gases absorbed by the reacting mixture is not by the vaporization of a gas, unlike the foaming by freon; therefore, it does not take away the reaction heat of the reacting mixture after injection. This permits the temperature rise of the reacting mixture and hence reduces the cure time.
  • the water content in the polyol mixture is limited to 0.4 wt%, so as to reduce the amount of the isocyanate to be consumed by water and hence to reduce the amount of the polyol mixture which will otherwise remain unreacted. This contributes to the improved physical properties (such as tensile strength and tear strength) of the resulting polyurethane foam.
  • the mold cavity should preferably be evacuated 6.65 kPa (50 Torr) or below, so as to help the gas bubbles to rupture in the reacting mixture in contact with the inner surface of the mold cavity. This makes the skin thick and eliminates the minute gas bubbles which will otherwise remain in the skin.
  • the reacting mixture is so formulated as to establish a proper reaction rate such that it cures to seal the vent as soon as it reaches the vent.
  • a reaction rate higher than that of the freon-containing reacting mixture. This contributes to improvement in production efficiency.
  • Evacuating the mold cavity offers another advantage in the case where a core metal is placed in the mold cavity. Even though the reacting mixture is subject to turbulence by the core metal, the turbulence under reduced pressure is less liable to cause defects such as pinholes, voids, and short shot. This permits one to select an adequate place for gating more freely and to reduce the number of vents.
  • the combination of an evacuated mold cavity and a core placed therein offers an advantage that an almost non-porous solid adhesive layer is formed on the core, because the core functions as a heat sink such that it absorbs reaction heat from the reacting mixture in contact with it, thereby stopping the reacting mixture from becoming viscous, and the less viscous reacting mixture releases gas from gas bubbles under reduced pressure.
  • the core is that of a steering wheel and at least the ring of the core is placed in the mold cavity.
  • the method of the present invention will prevent defects (such as weld line, pinholes, voids, and short shot) from occurring at the point where the flows of the reacting mixture meet one another.
  • the apparatus for producing an integral skin polyurethane foam has a vacuum chamber communicating with the mold cavity through the vent.
  • This vacuum chamber functions as an accumulator.
  • the vacuum chamber prevents the pressure in the mold cavity from increasing as the reacting mixture expands after injection.
  • the apparatus has a sight glass which makes the vicinity of the vent hole visible from the outside of the vacuum chamber.
  • the sight glass permits one to confirm the blowing off of the reacting mixture from the vent hole and to observe the reacting mixture expand, with the vacuum chamber kept closed.
  • FIG. 1 An embodiment of the present invention in the production of a steering wheel pad will be described with reference to Figs. 1 to 5.
  • This example employs an apparatus which is made up of (a) a split mold 1, (b) a vacuum chamber 11 arranged in the mold 1, (c) a vacuum pump 20 to evacuate the vacuum chamber 11, and (d) an injecting mechanism 21 which is attached to the vacuum chamber 11 and is intended to inject the reacting mixture into the cavity 4 of the mold 1.
  • a split mold 1 a vacuum chamber 11 arranged in the mold 1
  • FIG. 1 to 5 An embodiment of the present invention in the production of a steering wheel pad will be described with reference to Figs. 1 to 5.
  • This example employs an apparatus which is made up of (a) a split mold 1, (b) a vacuum chamber 11 arranged in the mold 1, (c) a vacuum pump 20 to evacuate the vacuum chamber 11, and (d) an injecting mechanism 21 which is attached to the vacuum chamber 11 and is intended to inject the reacting mixture into the cavity 4 of the mold 1.
  • the mold 1 is made up of a stationary half 2 and a movable half 3, which form a cavity 4 when closed.
  • the split molds In the PL (parting line) surface 2a of the stationary half 2 and the PL surface 3a of the movable half 3, the split molds have grooves which form a sprue 6, runner 7, and gate 8 through which the reacting material is injected into the cavity 4.
  • This clearance functions as an air vent land for venting (mentioned later).
  • a vent hole 5 is formed at that position L of the stationary half 2 where the filling of the cavity with the reacting mixture completes.
  • the vent hole 5 is usually 1-10 mm in diameter. With a diameter smaller than 1 mm, the vent hole 5 does not perform venting as desired, with the final filling position of the reacting mixture fluctuating. With a diameter larger than 10 mm, the vent hole 5 leaves a noticeable vent mark which makes the molded article look poor.
  • the vent hole 5 in this example is a straight one, 15 mm long and 3 mm in diameter.
  • the mold 1 may be made of aluminum or electroformed for economy, because it merely needs to withstand a foaming pressure, which is usually 50-500 kPa.
  • the vacuum chamber 11 is made up of an upper casing 12 to which the stationary half 2 is fixed and a lower casing 13 to which the movable half 3 is fixed.
  • the mating surface of the lower casing 13 is provided with a sealing O-ring 14, which makes the closed vacuum chamber 11 airtight.
  • the lower casing 13 is also provided with a suction port 16, which is connected to a vacuum pump 20 through a suction hose 15 and a leak valve 17, as shown in Fig. 5.
  • the vacuum chamber 11 in this example is constructed such that it accommodates the mold 1, forming a space K therein.
  • the injection mechanism 21, as shown in Fig. 5. is made up of a storage tank 25 for the polyol mixture, a storage tank 26 for the isocyanate, a mixing head 22, and two circuits 29, each connecting the storage tank and the head through a high-pressure pump 27 and filters 28.
  • This construction permits the mixing and circulation of the polyol mixture and isocyanate.
  • the mixing head 22 is provided with an injection nozzle 23 which can be connected to the sprue 6 of the mold 1 through O-rings 24.
  • the reacting mixture used in this example is composed of the above-mentioned polyol mixture and isocyanate.
  • the reacting mixture contains substantially no blowing agent deliberately added, with the water contain in the polyol mixture limited to no more than 0.4 wt%.
  • the temperature of the reacting mixture is higher than that of the conventional fleon-containing reacting mixture.
  • the polyol mixture is kept at about 40-50°C and the isocyanate is kept at about 25-30°C in this example, whereas the polyol mixture and isocyanate are both kept at about 25-30°C in the conventional freon-based foaming.
  • the freon-free reacting mixture in this example is more viscous than the conventional fleon-containing one; this disadvantage is eliminated by raising the temperature.
  • the molding apparatus has many parts common to that in the first example. Basically, it is constructed of a mold 1, a vacuum chamber 11, vacuum pump 20, and a injecting mechanism 21. Those parts common to that in the first example are indicated by like reference numbers in Figs. 6 to 11, and their description is not repeated except for the supplementary description that follows.
  • the core 42 of the steering wheel 41 is composed of a boss, a ring, and spokes connecting the boss and ring.
  • the mold 1 is intended to form the covering 43 around the ring and spokes of the core 42.
  • the mold 1 is composed of an upper stationary half 2 and a lower movable half 3. They have grooves 4a, which form a circular cavity 4 when they are closed. At the center of the cross-section of the cavity 4 is placed the core 42 (including the entire ring and a part of the spoke).
  • a gate 8 opens on the outer periphery of the groove 4a (the left side in Fig. 6). Upon injection into the cavity 4 through the gate 8, the reacting mixture M flows in two directions in the cavity 4 and the two flows meet at position L (at the right side in Fig. 6) where the filling of the cavity is completed.
  • a vent hole 5 through which the cavity 4 communicates with the space in the vacuum chamber 11.
  • the lower casing 13 of the vacuum chamber 11 is provided with a sight glass 51 which makes the vicinity of the vent hole 5 visible from the outside of the vacuum chamber 11, as shown in Figs. 9 and 10.
  • the sight glass 51 is made up of an opening 52 formed in the lower casing 13, a transparent plate 54 of glass or plastics which is pressed against the inside of the lower casing 13, with a seal ring 53 placed between them, so as to close the opening 52 from the inside, and a frame 56 which is fastened to the lower casing 13 by bolts 55 such that it presses the periphery of the transparent plate 54. It is desirable to place a gasket 57 between the frame 56 and the transparent plate 54 and between the frame 54 and the lower casing 13.
  • the stationary half 2 and the upper casing 12 are integrally constructed, and the movable half 3 and the lower casing 13 are also integrally constructed.
  • the lower casing 13 is connected to a hydraulic cylinder ram (not shown), so that it is raised and lowered as the mold is closed and opened. At the time of mold closing, the lower casing 13 is raised until its periphery comes into contact with the periphery of the upper casing 12.
  • the reacting mixture used in this example is composed of a polyol mixture and an isocyanate. It contains substantially no blowing agent deliberately added, and the water content in the polyol mixture is limited to less than 0.4 wt%.
  • the temperature of the reacting mixture is set higher than that of the conventional freon-containing reacting mixture.
  • Another advantage in this example is that the covering 43 firmly adheres to the ring of the core 42 owing to the solid adhesive layer 47.
  • the water content in the polyol mixture is limited to less than 0. 4 wt%, as mentioned above.
  • the following experiment was carried out.
  • Three reacting mixtures containing no freon were prepared according to the formulation shown in Table 1, with the water content in the polyol mixture limited to 0.13 wt%, 0.35 wt%, and 0.54 wt%.
  • Each of the reacting mixtures was made into the covering of the steering wheel under the molding conditions shown in Table 2. The covering was tested for physical properties.
  • a reacting mixture containing freon was prepared according to the formulation shown in Table 1, with the water content in the polyol mixture limited to 0.22 wt%.
  • the reacting mixture was made into the covering of the steering wheel under the conventional molding conditions shown in Table 2.
  • the covering was tested for physical properties.
  • the covering of the steering wheel produced as mentioned above was tested for tensile strength and tear strength at room temperature using a test piece cut out of the highly expanded core part. The results of the test are shown in Fig. 13 (tensile strength) and Fig. 14 (tear strength). It is noted that the polyurethane foam in this example is superior in tensile strength and tear strength to the conventional freon-based one, even in the case where the water content in the polyol mixture is 0.54 wt%. It is also noted that a pronounced effect is obtained when the water content in the polyol mixture is lower than 0.4 wt%.
  • Example 2 In order to see how the pressure in the cavity affects the thickness of the skin in Example 2, a reacting mixture containing no freon was prepared according to the formulation shown in Table 1, with the water content in the polyol mixture limited to 0.35 wt%, and the reacting mixture was made into the covering of the steering wheel under the molding conditions shown in Table 2, with the pressure in the cavity adjusted to 0.665, 1.596, 1.995, 2.660, 3.990, 6.650 and 13.3 kPa (5, 12, 15, 20, 30, 50, and 100 Torr). The covering was tested for the thickness of the skin. The results are shown in Fig. 15. It is noted that the thickness of the skin steeply increases when the pressure in the cavity is 6.65 kPa (50 Torr) or below.
  • the sectional photomicrographs showing the covering of the steering wheel produced in this experiment are shown in Figs. 17 to 23.
  • the covering of the steering wheel shown in Figs. 17 to 23 was produced with the pressure in the cavity adjusted respectively to 0.665, 1.596, 1.995, 2.660, 3.990, 6.650 and 13.3 kPa (5, 12, 15, 20, 30, 50, and 100 Torr).
  • the sectional photomicrograph, showing the covering of the steering wheel produced in the conventional fleon-based foaming under the conventional molding conditions shown in Tables 1 and 2 is shown in Fig. 24.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biodiversity & Conservation Biology (AREA)
  • Environmental & Geological Engineering (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
  • Moulds For Moulding Plastics Or The Like (AREA)
  • Molding Of Porous Articles (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)

Claims (6)

  1. Procédé de production d'une mousse en polyuréthanne à peau intégrée dans une cavité de moule qui comprend :
    (1) la mise de la cavité du moule sous vide pour réduire sa pression jusqu'à une pression barométrique prédéfinie;
    (2) l'injection, dans la cavité du moule où le vide a été fait, d'un mélange réactionnel, formant des uréthannes, contenant un mélange de polyols et ne contenant pratiquement pas d'agent moussant de petites quantités de gaz étant présentes à l'origine dans ledit mélange réactionnel et étant absorbées inévitablement par lui pendant son pompage; et
    (3) l'abandon du mélange réactionnel formant des uréthannes pour qu'il réagisse et s'expanse par suite de l'expansion desdits gaz absorbés par ledit mélange réactionnel, dans la cavité du moule où le vide a été fait, pour formation de la mousse de polyuréthanne à peau intégrée.
  2. Procédé pour la production d'une mousse de polyuréthanne à peau intégrée telle que définie dans la revendication 1, dans lequel le vide est fait dans la cavité du moule jusqu'à 6,65 kPa (50 torr) ou au-dessous.
  3. Procédé pour la production d'une mousse de polyuréthanne à peau intégrée telle que définie dans la revendication 1, dans lequel le mélange réactionnel a une vitesse de réaction contrôlée de telle façon que, quand le mélange réactionnel injecté atteint un orifice d'évent du moule, la partie du mélange réactionnel qui est en contact avec ledit orifice d'évent durcit pour fermer ledit orifice d'évent.
  4. Procédé pour la production d'une mousse de polyuréthanne à peau intégrée telle que définie dans la revendication 1, dans lequel une préforme métallique est préalablement placée dans la cavité du moule.
  5. Procédé pour la production d'une mousse de polyuréthanne à peau intégrée telle que définie dans la revendication 4, dans lequel ladite préforme métallique est celle d'un volant composé d'un moyeu, d'une jante et de rayons reliant le moyeu et la jante et dans lequel au moins la jante de la préforme métallique est placée dans la cavité du moule.
  6. Procédé tel que défini dans la revendication 1, dans lequel ledit mélange de polyols contient moins de 0.4 % d'eau en masse.
EP92116164A 1991-09-26 1992-09-22 Méthode pour la production d'un produit moulé de mousse de polyuréthane à peau intégrale Expired - Lifetime EP0534358B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP277285/91 1991-09-26
JP3277285A JP2518481B2 (ja) 1991-09-26 1991-09-26 自己スキン層付きポリウレタンフォ―ムの製造方法及び製造装置

Publications (2)

Publication Number Publication Date
EP0534358A1 EP0534358A1 (fr) 1993-03-31
EP0534358B1 true EP0534358B1 (fr) 1996-12-04

Family

ID=17581404

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92116164A Expired - Lifetime EP0534358B1 (fr) 1991-09-26 1992-09-22 Méthode pour la production d'un produit moulé de mousse de polyuréthane à peau intégrale

Country Status (4)

Country Link
US (1) US5449698A (fr)
EP (1) EP0534358B1 (fr)
JP (1) JP2518481B2 (fr)
DE (1) DE69215628T2 (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2746024B2 (ja) * 1992-10-30 1998-04-28 豊田合成株式会社 Rimポリウレタン二色成形方法
JP2936929B2 (ja) * 1992-12-22 1999-08-23 豊田合成株式会社 真空箱付き成形装置
US5633289A (en) * 1993-03-16 1997-05-27 Toyoda Gosei Co., Ltd. Process for molding an integral skin foam and a polyurethane material for molding the same
DE4447494C2 (de) * 1993-04-30 1998-05-28 Toyoda Gosei Kk Verfahren zum Formschäumen von Integralschaum
DE4412976C2 (de) * 1993-04-30 1997-12-11 Toyoda Gosei Kk Verfahren zum Formschäumen von Integralschaum
JP2982564B2 (ja) * 1993-06-19 1999-11-22 豊田合成株式会社 インテグラルスキンフォームの成形方法
JPH0940906A (ja) * 1995-07-28 1997-02-10 Toyoda Gosei Co Ltd インテグラルスキンフォーム成形品
US6352659B1 (en) * 1997-05-30 2002-03-05 Woodbridge Foam Corporation Vented mold and method for producing a molded article
DE60007209T2 (de) 1999-03-31 2005-08-11 Toyoda Gosei Co., Ltd., Nishikasugai Verfahren zur Herstellung von Polyurethan-Formteilen
DE60007050T2 (de) 1999-09-29 2004-06-03 Toyoda Gosei Co., Ltd., Nishikasugai IMC-Verfahren
JP3780770B2 (ja) * 1999-09-30 2006-05-31 豊田合成株式会社 インテグラルスキンフォームの成形方法及び成形用ポリウレタン材料
US7731766B2 (en) * 2004-03-15 2010-06-08 Samsung Sdi Co., Ltd. Molding a battery
AU2005224247B2 (en) * 2004-03-23 2010-04-01 Sintokogio, Ltd. Casting mold forming apparatus and metal mold unit for use therein
US20070266613A1 (en) * 2006-05-19 2007-11-22 Nelson Barry J Decoy portions and decoys comprising rigid polyurethane, and related methods
MX2010010481A (es) * 2008-03-26 2011-05-25 Delta Tooling Company Metodo para la fabricacion de un articulo de nucleo espumado clase "a".
WO2009120838A2 (fr) * 2008-03-26 2009-10-01 Delta Tooling Company Outillage de moule interchangeable
US7846533B2 (en) * 2008-03-26 2010-12-07 Hendrickson Usa, L.L.C. Molded thermoplastic articles
DE102008041832B4 (de) * 2008-09-05 2013-03-21 Airbus Operations Gmbh Vorrichtung und Verfahren
CA2743516A1 (fr) * 2008-11-21 2010-05-27 Bayer Materialscience Ag Materiau multicouche en matiere plastique refractaire
WO2020008239A1 (fr) 2018-07-04 2020-01-09 Bosch Car Multimedia Portugal, S.A. Plateau universel pour l'accueil et le transport de dispositifs sensibles à la décharge électrostatique basés sur une mousse de peau intégrée
WO2022144579A1 (fr) 2020-12-30 2022-07-07 Universidade Do Minho Emballage polymère injecté pour un produit sensible ou fragile et procédé associé
CN120916879A (zh) * 2023-01-19 2025-11-07 莫西埃特有限责任公司 用于优化注射成型参数、配方和模具结构的装置和方法

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1813298A1 (de) * 1968-12-07 1970-06-25 Schlebach Hydraulik Georg Schl Formentlueftung fuer Reaktions-Spritzguss (z.B. Polyurethan)
DE2212609A1 (de) * 1972-03-16 1973-10-04 Ver Foerderung Inst Kunststoff Einrichtung zum entlueften von formwerkzeugen beim herstellen von formteilen aus schaumkunststoffen
GB1407244A (en) * 1972-08-15 1975-09-24 Ici Ltd Polyurethane foams
US3970732A (en) * 1973-09-26 1976-07-20 Kimball International, Inc. Method of molding rigid foamed polyurethane articles
DE2365203B2 (de) * 1973-12-31 1977-02-03 Dynamit Nobel Ag, 5210 Troisdorf Herstellen von mehrschichtigen bahnen, platten, formteilen
US4206170A (en) * 1975-05-06 1980-06-03 The Goodyear Tire & Rubber Company Method of molding a torus shaped article
FR2428519A1 (fr) * 1978-06-13 1980-01-11 Ameublement Ind Et Tech Bouchon pour trou de coulee de matiere expansee dans un moule
JPS5563238A (en) * 1978-11-07 1980-05-13 Matsushita Refrig Co Device for molding hard polyurethane foamed article
JPS5563237A (en) * 1978-11-07 1980-05-13 Matsushita Refrig Co Device for molding hard polyurethane foamed article
JPS56111648A (en) * 1980-02-07 1981-09-03 Tokyo Seat Kk Manufacture of porous resin product
WO1982000297A1 (fr) * 1980-07-15 1982-02-04 J Blackwell Production d'un materiau de mousse de plastique synthetique
GB2092509A (en) * 1981-02-11 1982-08-18 Ici Ltd Moulding apparatus and method of manufacturing foamed plastics articles.
AT374206B (de) * 1982-11-15 1984-03-26 Hirsch Kurt Verfahren und vorrichtung zum vorschaeumen von kunststoffen
DE3310677C1 (de) * 1983-03-24 1984-03-15 Elastogran Maschinenbau GmbH, 2844 Lemförde Geteilte Giessform fuer Mehrkomponentenkunststoffe,insbesondere Polyurethane
US4579700A (en) * 1983-11-07 1986-04-01 Union Carbide Corporation Novel process for making flexible polyurethane cellular products including a novel cell opening technique
US4572865A (en) * 1983-12-05 1986-02-25 The Celotex Corporation Faced foam insulation board and froth-foaming method for making same
DE3407931A1 (de) * 1984-03-03 1985-09-05 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von formkoerpern auf basis von harnstoffgruppen aufweisenden polyurethanen
US4517313A (en) * 1984-04-11 1985-05-14 Abbott Laboratories Method of making polyurethane foam
GB8516617D0 (en) * 1985-07-01 1985-08-07 Ici Plc Reinforced shaped article
US4909972A (en) * 1985-12-02 1990-03-20 Britz Johannes H Method and apparatus for making a solid foamed tire core
JPS62164709A (ja) * 1986-01-14 1987-07-21 Human Ind Corp ポリウレタンフオ−ムの製造方法
CA1290895C (fr) * 1986-12-25 1991-10-15 Sadao Kumasaka Methode et appareil de production de mousse polyurethanne
JPS63268624A (ja) * 1987-04-27 1988-11-07 Tokyo Seat Kk 多孔質樹脂材の製造方法及び多孔質複合基材の製造方法
JPS645528A (en) * 1987-06-29 1989-01-10 Colin Electronics Blood pressure monitor apparatus
NZ226008A (en) * 1987-09-21 1990-11-27 Ici Plc Process for manufacture of polyurethane foams using methylene diphenyl isocyanates and optionally water as blowing agent
FR2634157B1 (fr) * 1988-07-15 1991-07-26 Casati Francois Procede et dispositif pour fabriquer par moulage des objets rembourres
JP2613441B2 (ja) * 1988-07-18 1997-05-28 トヨタ自動車株式会社 発泡ポリウレタンの製法
US4906672A (en) * 1988-07-29 1990-03-06 Pmc, Inc. Blowing agents for polyurethane foam
US5132329A (en) * 1990-04-05 1992-07-21 Basf Corporation Integral skin polyurethane foam
EP0451559A3 (en) * 1990-04-05 1992-11-25 Basf Corporation (A Delaware Corp.) Integral skin polyurethane foam
JPH07102583B2 (ja) * 1990-06-12 1995-11-08 豊田合成株式会社 ポリウレタン発泡体の成形方法及び成形装置
US5166183A (en) * 1991-04-16 1992-11-24 Miles Inc. Water-blown integral skin polyurethane foams
IL144010A (en) * 2001-06-26 2006-04-10 Engines Pdm Ltd Universal diagnostic method and system for engines

Also Published As

Publication number Publication date
DE69215628D1 (de) 1997-01-16
EP0534358A1 (fr) 1993-03-31
US5449698A (en) 1995-09-12
JPH0671769A (ja) 1994-03-15
JP2518481B2 (ja) 1996-07-24
DE69215628T2 (de) 1997-04-24

Similar Documents

Publication Publication Date Title
EP0534358B1 (fr) Méthode pour la production d'un produit moulé de mousse de polyuréthane à peau intégrale
EP0461522B1 (fr) Procédé pour le moulage d'une masse de polyuréthane
US5476619A (en) Process for molding an integral skin foam using an evacuated mold cavity
US4285893A (en) Method and device for forming plastic cellular material in a mold from a foamable liquid reaction mixture
US3901958A (en) Method and apparatus for forming foamed plastic articles
AU740938B2 (en) Process for molding an integral skin foam and a polyurethane formulation for molding the same
US5633289A (en) Process for molding an integral skin foam and a polyurethane material for molding the same
JP2936929B2 (ja) 真空箱付き成形装置
EP0781643A2 (fr) Procédé de moulage par injection - réaction pour la fabrication des pièces bicolorées en polyuréthanes
US3878279A (en) System for the manufacture of foamed reproductions of articles
JPH0825230B2 (ja) 内周面上の発泡セルを破裂させた中空成形品及びその製造方法
US6361723B1 (en) Process and device for manufacturing polyurethane foam moldings
US6383423B1 (en) Process for producing polyurethane molded articles
JPH06287266A (ja) 成形用ポリウレタン材料
JP2806200B2 (ja) インテグラルスキンフォームの成形方法及び成形用ポリウレタン材料
JP2806204B2 (ja) インテグラルスキンフォームの成形方法及び成形用ポリウレタン材料
GB2362889A (en) Polyurethane formulation for moulding
US6981861B2 (en) Foaming mold using hollow tubes
JPH08108444A (ja) 構造反応射出成形装置及び構造反応射出成形方法
JP4120088B2 (ja) Rimポリウレタン成形方法及びポリウレタン成形品
JPH06315942A (ja) インテグラルスキンフォームの成形方法及び成形用ポリウレタン材料
JPH06315943A (ja) インテグラルスキンフォームの成形方法
JPH071478A (ja) インテグラルスキンフォームの成形方法及び成形用ポリウレタン材料
JPH11277575A (ja) 発泡樹脂成形品の成形方法
JP2003001642A (ja) 発泡成形体の製造方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19920922

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB

17Q First examination report despatched

Effective date: 19941010

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB

REF Corresponds to:

Ref document number: 69215628

Country of ref document: DE

Date of ref document: 19970116

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20090916

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20090917

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20091012

Year of fee payment: 18

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20100922

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20110531

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 69215628

Country of ref document: DE

Effective date: 20110401

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110401

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20100930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20100922